Clinical Research Trials Archive – Closed Trials

This is our archive of closed clinical trials, which means that they are no longer accepting new participants or have been concluded. Once a research facility has chosen to close the study, it is sorted into the GPS archive by indication. If you are interested in enrolling in a clinical trial, then please browse our list of active clinical studies.

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We've found
31,654
archived clinical trials in
Cardiology

Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated:  12/31/1969
University of Kansas Hospital
mi
from
Kansas City, KA
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated: 12/31/1969
University of Kansas Hospital
mi
from
Kansas City, KA
Click here to add this to my saved trials
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated:  12/31/1969
Cardiovascular Institute of the South/Terrebonne General
mi
from
Houma, LA
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated: 12/31/1969
Cardiovascular Institute of the South/Terrebonne General
mi
from
Houma, LA
Click here to add this to my saved trials
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated:  12/31/1969
Beth Israel Deaconess Medical Center
mi
from
Boston, MA
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated: 12/31/1969
Beth Israel Deaconess Medical Center
mi
from
Boston, MA
Click here to add this to my saved trials
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated:  12/31/1969
St John Hospital & Medical Center
mi
from
Detroit, MI
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated: 12/31/1969
St John Hospital & Medical Center
mi
from
Detroit, MI
Click here to add this to my saved trials
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated:  12/31/1969
Detroit Medical Center Cardiovascular Institute
mi
from
Detroit, MI
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated: 12/31/1969
Detroit Medical Center Cardiovascular Institute
mi
from
Detroit, MI
Click here to add this to my saved trials
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated:  12/31/1969
Spectrum Health Hospitals
mi
from
Grand Rapids, MI
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated: 12/31/1969
Spectrum Health Hospitals
mi
from
Grand Rapids, MI
Click here to add this to my saved trials
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated:  12/31/1969
Morristown Memorial Hospital
mi
from
Morristown, NJ
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated: 12/31/1969
Morristown Memorial Hospital
mi
from
Morristown, NJ
Click here to add this to my saved trials
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated:  12/31/1969
North Shore University Hospital/ Long Island Jewish Hospital
mi
from
Manhasset, NY
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated: 12/31/1969
North Shore University Hospital/ Long Island Jewish Hospital
mi
from
Manhasset, NY
Click here to add this to my saved trials
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated:  12/31/1969
Lenox Hill Hospital
mi
from
New York, NY
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated: 12/31/1969
Lenox Hill Hospital
mi
from
New York, NY
Click here to add this to my saved trials
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated:  12/31/1969
Mount Sinai Hospital
mi
from
New York, NY
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated: 12/31/1969
Mount Sinai Hospital
mi
from
New York, NY
Click here to add this to my saved trials
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated:  12/31/1969
St. Francis Hospital
mi
from
Roslyn, NY
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated: 12/31/1969
St. Francis Hospital
mi
from
Roslyn, NY
Click here to add this to my saved trials
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated:  12/31/1969
Duke Univ Med Ctr
mi
from
Durham, NC
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated: 12/31/1969
Duke Univ Med Ctr
mi
from
Durham, NC
Click here to add this to my saved trials
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated:  12/31/1969
Riverside Methodist Hospital
mi
from
Columbus, OH
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated: 12/31/1969
Riverside Methodist Hospital
mi
from
Columbus, OH
Click here to add this to my saved trials
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated:  12/31/1969
The Ohio State University Medical Center - The Richard M. Ross Heart Hospital
mi
from
Columbus, OH
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated: 12/31/1969
The Ohio State University Medical Center - The Richard M. Ross Heart Hospital
mi
from
Columbus, OH
Click here to add this to my saved trials
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated:  12/31/1969
Geisinger Medical Center
mi
from
Danville, PA
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated: 12/31/1969
Geisinger Medical Center
mi
from
Danville, PA
Click here to add this to my saved trials
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated:  12/31/1969
Pinnacle Health
mi
from
Harrisburg, PA
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated: 12/31/1969
Pinnacle Health
mi
from
Harrisburg, PA
Click here to add this to my saved trials
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated:  12/31/1969
University of Pittsburgh Medical Center
mi
from
Pittsburgh, PA
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated: 12/31/1969
University of Pittsburgh Medical Center
mi
from
Pittsburgh, PA
Click here to add this to my saved trials
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated:  12/31/1969
Vanderbilt University Medical Center
mi
from
Nashville, TN
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated: 12/31/1969
Vanderbilt University Medical Center
mi
from
Nashville, TN
Click here to add this to my saved trials
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated:  12/31/1969
Baylor Heart and Vascular Hospital
mi
from
Dallas, TX
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated: 12/31/1969
Baylor Heart and Vascular Hospital
mi
from
Dallas, TX
Click here to add this to my saved trials
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated:  12/31/1969
Texas Heart Institute - St. Luke's Episcopal Hospital
mi
from
Houston, TX
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated: 12/31/1969
Texas Heart Institute - St. Luke's Episcopal Hospital
mi
from
Houston, TX
Click here to add this to my saved trials
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated:  12/31/1969
The Methodist Hospital - The Methodist DeBakey Heart & Vascular Center
mi
from
Houston, TX
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated: 12/31/1969
The Methodist Hospital - The Methodist DeBakey Heart & Vascular Center
mi
from
Houston, TX
Click here to add this to my saved trials
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated:  12/31/1969
Inova Fairfax Hospital
mi
from
Falls Church, VA
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated: 12/31/1969
Inova Fairfax Hospital
mi
from
Falls Church, VA
Click here to add this to my saved trials
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated:  12/31/1969
Providence Sacred Heart Medical Center
mi
from
Spokane, WA
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated: 12/31/1969
Providence Sacred Heart Medical Center
mi
from
Spokane, WA
Click here to add this to my saved trials
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated:  12/31/1969
St. Luke's Medical Center - Aurora Health Care
mi
from
Milwaukee, WI
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated: 12/31/1969
St. Luke's Medical Center - Aurora Health Care
mi
from
Milwaukee, WI
Click here to add this to my saved trials
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated:  12/31/1969
Johns Hopkins Hospital
mi
from
Baltimore, MD
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated: 12/31/1969
Johns Hopkins Hospital
mi
from
Baltimore, MD
Click here to add this to my saved trials
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated:  12/31/1969
University of Michigan Health Systems
mi
from
Ann Arbor, MI
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated: 12/31/1969
University of Michigan Health Systems
mi
from
Ann Arbor, MI
Click here to add this to my saved trials
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated:  12/31/1969
NYU Langone Medical Center
mi
from
New York, NY
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated: 12/31/1969
NYU Langone Medical Center
mi
from
New York, NY
Click here to add this to my saved trials
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated:  12/31/1969
University Hospitals at Case Medical Center
mi
from
Cleveland, OH
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated: 12/31/1969
University Hospitals at Case Medical Center
mi
from
Cleveland, OH
Click here to add this to my saved trials
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated:  12/31/1969
Wake Forest University Baptist Medical Center
mi
from
Winston-Salem, NC
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated: 12/31/1969
Wake Forest University Baptist Medical Center
mi
from
Winston-Salem, NC
Click here to add this to my saved trials
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated:  12/31/1969
Washington Hospital Center / Georgetown Hospital
mi
from
Washington,
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated: 12/31/1969
Washington Hospital Center / Georgetown Hospital
mi
from
Washington,
Click here to add this to my saved trials
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated:  12/31/1969
University of Vermont Medical Center
mi
from
Burlington, VT
Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement
Medtronic CoreValve® Continued Access Study
Status: Enrolling
Updated: 12/31/1969
University of Vermont Medical Center
mi
from
Burlington, VT
Click here to add this to my saved trials
Dietary Salt in Postural Tachycardia Syndrome
Dietary Salt in Postural Tachycardia Syndrome
Status: Enrolling
Updated:  12/31/1969
Vanderbilt University Medical Center
mi
from
Nashville, TN
Dietary Salt in Postural Tachycardia Syndrome
Dietary Salt in Postural Tachycardia Syndrome
Status: Enrolling
Updated: 12/31/1969
Vanderbilt University Medical Center
mi
from
Nashville, TN
Click here to add this to my saved trials
Effect of Dietary Sodium Intake on Vascular Endothelium
A Pilot Study of the Effect of Dietary Sodium Intake on Assessments of Vascular Endothelium
Status: Enrolling
Updated:  12/31/1969
Vanderbilt University Medical Center
mi
from
Nashville, TN
Effect of Dietary Sodium Intake on Vascular Endothelium
A Pilot Study of the Effect of Dietary Sodium Intake on Assessments of Vascular Endothelium
Status: Enrolling
Updated: 12/31/1969
Vanderbilt University Medical Center
mi
from
Nashville, TN
Click here to add this to my saved trials
Efficacy & Safety Trial of Intravitreal Injections Combined With PRP for CSME Secondary to Diabetes Mellitus (DAVE)
A Phase I/II, Randomized, Study for Diabetic Macular Edema Using 0.3mg Ranibizumab Combined With Targeted PRP Monthly for 4 Months,Then PRN vs. 0.3mg Ranibizumab 4 Months Monotherapy, Then as Needed(DME-AntiVEgf) DAVE
Status: Enrolling
Updated:  12/31/1969
Retina Consultants of Houston
mi
from
Houston, TX
Efficacy & Safety Trial of Intravitreal Injections Combined With PRP for CSME Secondary to Diabetes Mellitus (DAVE)
A Phase I/II, Randomized, Study for Diabetic Macular Edema Using 0.3mg Ranibizumab Combined With Targeted PRP Monthly for 4 Months,Then PRN vs. 0.3mg Ranibizumab 4 Months Monotherapy, Then as Needed(DME-AntiVEgf) DAVE
Status: Enrolling
Updated: 12/31/1969
Retina Consultants of Houston
mi
from
Houston, TX
Click here to add this to my saved trials
Efficacy & Safety Trial of Intravitreal Injections Combined With PRP for CSME Secondary to Diabetes Mellitus (DAVE)
A Phase I/II, Randomized, Study for Diabetic Macular Edema Using 0.3mg Ranibizumab Combined With Targeted PRP Monthly for 4 Months,Then PRN vs. 0.3mg Ranibizumab 4 Months Monotherapy, Then as Needed(DME-AntiVEgf) DAVE
Status: Enrolling
Updated:  12/31/1969
Retina Consultants of Houston
mi
from
Katy, TX
Efficacy & Safety Trial of Intravitreal Injections Combined With PRP for CSME Secondary to Diabetes Mellitus (DAVE)
A Phase I/II, Randomized, Study for Diabetic Macular Edema Using 0.3mg Ranibizumab Combined With Targeted PRP Monthly for 4 Months,Then PRN vs. 0.3mg Ranibizumab 4 Months Monotherapy, Then as Needed(DME-AntiVEgf) DAVE
Status: Enrolling
Updated: 12/31/1969
Retina Consultants of Houston
mi
from
Katy, TX
Click here to add this to my saved trials
Efficacy & Safety Trial of Intravitreal Injections Combined With PRP for CSME Secondary to Diabetes Mellitus (DAVE)
A Phase I/II, Randomized, Study for Diabetic Macular Edema Using 0.3mg Ranibizumab Combined With Targeted PRP Monthly for 4 Months,Then PRN vs. 0.3mg Ranibizumab 4 Months Monotherapy, Then as Needed(DME-AntiVEgf) DAVE
Status: Enrolling
Updated:  12/31/1969
Retina Consultants of Houston
mi
from
The Woodlands, TX
Efficacy & Safety Trial of Intravitreal Injections Combined With PRP for CSME Secondary to Diabetes Mellitus (DAVE)
A Phase I/II, Randomized, Study for Diabetic Macular Edema Using 0.3mg Ranibizumab Combined With Targeted PRP Monthly for 4 Months,Then PRN vs. 0.3mg Ranibizumab 4 Months Monotherapy, Then as Needed(DME-AntiVEgf) DAVE
Status: Enrolling
Updated: 12/31/1969
Retina Consultants of Houston
mi
from
The Woodlands, TX
Click here to add this to my saved trials
Effect of ACP-501 on Safety, Tolerability, Pharmacokinetics and Pharmacodynamics in Subjects With Coronary Artery Disease
An Intravenous, Open-label, Single-dose Escalation Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of rhLCAT in Subjects With Coronary Artery Disease
Status: Enrolling
Updated:  12/31/1969
Cardiovascular and Pulmonary Branch (CPB) of NIH
mi
from
Bethesda, MD
Effect of ACP-501 on Safety, Tolerability, Pharmacokinetics and Pharmacodynamics in Subjects With Coronary Artery Disease
An Intravenous, Open-label, Single-dose Escalation Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of rhLCAT in Subjects With Coronary Artery Disease
Status: Enrolling
Updated: 12/31/1969
Cardiovascular and Pulmonary Branch (CPB) of NIH
mi
from
Bethesda, MD
Click here to add this to my saved trials
Quadripolar Pacing Post Approval Study
Quadripolar Pacing Post Approval Study
Status: Enrolling
Updated:  12/31/1969
Cardiology PC
mi
from
Birmingham, AL
Quadripolar Pacing Post Approval Study
Quadripolar Pacing Post Approval Study
Status: Enrolling
Updated: 12/31/1969
Cardiology PC
mi
from
Birmingham, AL
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Quadripolar Pacing Post Approval Study
Quadripolar Pacing Post Approval Study
Status: Enrolling
Updated:  12/31/1969
Heart Center Research, LLC/Research Center
mi
from
Huntsville, AL
Quadripolar Pacing Post Approval Study
Quadripolar Pacing Post Approval Study
Status: Enrolling
Updated: 12/31/1969
Heart Center Research, LLC/Research Center
mi
from
Huntsville, AL
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Quadripolar Pacing Post Approval Study
Quadripolar Pacing Post Approval Study
Status: Enrolling
Updated:  12/31/1969
Southeastern Cardiology Consultants PC
mi
from
Montgomery, AL
Quadripolar Pacing Post Approval Study
Quadripolar Pacing Post Approval Study
Status: Enrolling
Updated: 12/31/1969
Southeastern Cardiology Consultants PC
mi
from
Montgomery, AL
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Quadripolar Pacing Post Approval Study
Quadripolar Pacing Post Approval Study
Status: Enrolling
Updated:  12/31/1969
Arizona Arrhythmia Research Center
mi
from
Phoenix, AZ
Quadripolar Pacing Post Approval Study
Quadripolar Pacing Post Approval Study
Status: Enrolling
Updated: 12/31/1969
Arizona Arrhythmia Research Center
mi
from
Phoenix, AZ
Click here to add this to my saved trials
Quadripolar Pacing Post Approval Study
Quadripolar Pacing Post Approval Study
Status: Enrolling
Updated:  12/31/1969
Washington Regional Medical Center
mi
from
Fayetteville, AR
Quadripolar Pacing Post Approval Study
Quadripolar Pacing Post Approval Study
Status: Enrolling
Updated: 12/31/1969
Washington Regional Medical Center
mi
from
Fayetteville, AR
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Quadripolar Pacing Post Approval Study
Quadripolar Pacing Post Approval Study
Status: Enrolling
Updated:  12/31/1969
Arkansas Heart Hospital
mi
from
Little Rock, AR
Quadripolar Pacing Post Approval Study
Quadripolar Pacing Post Approval Study
Status: Enrolling
Updated: 12/31/1969
Arkansas Heart Hospital
mi
from
Little Rock, AR
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Quadripolar Pacing Post Approval Study
Quadripolar Pacing Post Approval Study
Status: Enrolling
Updated:  12/31/1969
Comprehensive Cardiovascular
mi
from
Bakersfield, CA
Quadripolar Pacing Post Approval Study
Quadripolar Pacing Post Approval Study
Status: Enrolling
Updated: 12/31/1969
Comprehensive Cardiovascular
mi
from
Bakersfield, CA
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Quadripolar Pacing Post Approval Study
Quadripolar Pacing Post Approval Study
Status: Enrolling
Updated:  12/31/1969
Scripps Green Hospital
mi
from
La Jolla, CA
Quadripolar Pacing Post Approval Study
Quadripolar Pacing Post Approval Study
Status: Enrolling
Updated: 12/31/1969
Scripps Green Hospital
mi
from
La Jolla, CA
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Quadripolar Pacing Post Approval Study
Quadripolar Pacing Post Approval Study
Status: Enrolling
Updated:  12/31/1969
USC Unversity Hospital
mi
from
Los Angeles, CA
Quadripolar Pacing Post Approval Study
Quadripolar Pacing Post Approval Study
Status: Enrolling
Updated: 12/31/1969
USC Unversity Hospital
mi
from
Los Angeles, CA
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Quadripolar Pacing Post Approval Study
Quadripolar Pacing Post Approval Study
Status: Enrolling
Updated:  12/31/1969
Fogarty Institute
mi
from
Mountain View, CA
Quadripolar Pacing Post Approval Study
Quadripolar Pacing Post Approval Study
Status: Enrolling
Updated: 12/31/1969
Fogarty Institute
mi
from
Mountain View, CA
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Quadripolar Pacing Post Approval Study
Quadripolar Pacing Post Approval Study
Status: Enrolling
Updated:  12/31/1969
Premier Cardiology, Inc.
mi
from
Newport Beach, CA
Quadripolar Pacing Post Approval Study
Quadripolar Pacing Post Approval Study
Status: Enrolling
Updated: 12/31/1969
Premier Cardiology, Inc.
mi
from
Newport Beach, CA
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Quadripolar Pacing Post Approval Study
Quadripolar Pacing Post Approval Study
Status: Enrolling
Updated:  12/31/1969
Cardiac Rhythm Specialists, Inc.
mi
from
Northridge, CA
Quadripolar Pacing Post Approval Study
Quadripolar Pacing Post Approval Study
Status: Enrolling
Updated: 12/31/1969
Cardiac Rhythm Specialists, Inc.
mi
from
Northridge, CA
Click here to add this to my saved trials
Quadripolar Pacing Post Approval Study
Quadripolar Pacing Post Approval Study
Status: Enrolling
Updated:  12/31/1969
St. Joseph Heritage Medical Group
mi
from
Orange, CA
Quadripolar Pacing Post Approval Study
Quadripolar Pacing Post Approval Study
Status: Enrolling
Updated: 12/31/1969
St. Joseph Heritage Medical Group
mi
from
Orange, CA
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